SASDEL3

The neutrophil cytosol factor 2 (p67phox) subunit of phagocyte NADPH oxidase

Data type: SASBDB experimental data Status: Published Curve type: Extrapolated to infinite dilution Last updated: 2020-08-28T15:27:52.342524+02:00
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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · The neutrophil cytosol factor 2 (p67phox) subunit of phagocyte NADPH oxidase

Concentration0.3 – 3.8 Buffer / pH20 mM HEPES, 50 mM NaCl, 1 mM EDTA, 2 mM DTT, 5% glycerol / 8.0
Experimental temperature4.0 Facility / beamlineLURE / D24
Wavelength0.1488 nmExposure200.0 s × 8

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Neutrophil cytosol factor 2
View sequence
GPLGSPNSARMSLVEAISLWNEGVLAADKKDWKGALDAFSAVQDPHSRICFNIGCMYTILKNMTEAEKAFTRSINRDKHLAVAYFQRGMLYYQTEKYDLAIKDLKEALIQLRGNQLIDYKILGLQFKLFACEVLYNIAFMYAKKEEWKKAEEQLALATSMKSEPRHSKIDKAMECVWKQKLYEPVVIPVGKLFRPNERQVAQLAKKDYLGKATVVASVVDQDSFSGFAPLQPQAAEPPPRPKTPEIFRALEGEAHRVLFGFVPETKEELQVMPGNIVFVLKKGNDNWATVMFNGQKGLVPCNYLEPVELRIHPQQQPQEESSPQSDIPAPPSSKAPGRPQLSPGQKQKEEPKEVKLSVPMPYTLKVHYKYTVVMKTQPGLPYSQVRDMVSKKLELRLEHTKLSYRPRDSNELVPLSEDSMKDAWGQVKNYCLTLWCENTVGDQGFPDEPKESEKADANNQTTEPQLKKGSQVEALFSYEATQPEDLEFQEGDIILVLSKVNEEWLEGESKGKVGIFPKVFVEDSATTDLESTRREV
proteinHomo sapiensP198781–526monomerMolecule count 160.666 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
1175[3]0.014831–0.33741 1/AHas uncertainty columnMissing 00sasbdb/entries/l3/sasdel3/source/SASDEL3.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)16.01.0Å
i0Guinier0.050.00061/cm
i0P(r)0.050880.00061/cm
mwExperimental62.4—kDa
mwGuinier I(0)60.46.0kDa
mwPorod75.3—kDa
porod_volumePorod113.0—ų
rgGuinier4.270.1Å
rgP(r)4.540.1Å

These values are reported by SASBDB; SAXSdb did not recalculate them from the experimental curve.

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3. Source Fits and Models Source Fits & Models

Fit 1 · BUNCH 08

χ²: 1.304CorMap p: 1e-06Unit: 1/A

p67phox in solution: Comparison of the experimental data (blue dots) with the calculated scattering pattern (red line) of the BUNCH model shown on the rightchi2=1.304. The ultimate adjustment shown here was performed using the program CRYSOL.

ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—atomicCustom in-house —63.06—Model Image

Fit 2 · EOM/GAJOE 2.1

χ²: 0.828CorMap p: 0.493356Unit: 1/A

The fitting to the experimental curve using EOM program. This good fit with our experimental intensities chi2=0.828) was obtained only when using the “compact” reconstructed linkers.

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4. Source File Index Source Files

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5. Experiment Description and Publication Experiment & Publication

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6. Complete Source Record Complete Source Record

The following content comes directly from the SASBDB entry. Missing values are shown as “—”; SAXSdb does not infer undeclared units.

Open the original SASBDB entry

Buffer and Sample Properties

Buffer name20 mM HEPES, 50 mM NaCl, 1 mM EDTA, 2 mM DTT, 5% glycerolBuffer concentration—
pH8.0Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2003-04-09Storage / measurement temperature4.0 / 4.0
Exposure time200.0Frames8
Wavelength0.1488Sample-to-detector distance1.378
SourceX-ray synchrotronDetectorLinear gas detector
Facility / beamlineLURE / D24 · Orsay, France
q range0.148 – 3.374Sample volume / flow rate— / —

Original SASBDB Plots

Experimental I(q)
Experimental I(q)
Experimental I(q), log-log
Experimental I(q), log-log
Guinier plot
Guinier plot
Kratky plot
Kratky plot
P(r) plot
P(r) plot

Downloadable Files

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full_entry_zip:source record and ZIP contents (6 items)
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All source fields (unfiltered)

Every source field is expanded here, including empty values, list members and fields already shown above.

summary.json:167 field values
Field pathRaw value
codeSASDEL3
statusPublished
type_of_curveExtrapolated to infinite dilution
angular_unit1/A
project.titleQuantitative live-cell imaging and 3D modeling reveal critical functional features in the cytosolic complex of phagocyte NADPH oxidase.
project.publication.titleQuantitative live-cell imaging and 3D modeling reveal critical functional features in the cytosolic complex of phagocyte NADPH oxidase.
project.publication.author_listZiegler CS, Bouchab L, Tramier M, Durand D, Fieschi F, Dupré-Crochet S, Mérola F, Nüße O, Erard M
project.publication.journalJ Biol Chem
project.publication.doi10.1074/jbc.RA118.006864
project.publication.pmid30630949
project.publication.published_date2019 Jan 10
project.statusreleased
project.submitted_date2018-08-28
project.released_date2019-01-16
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDEL3.out
intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDEL3.dat
intensities_log_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDEL3_dat_img.png
intensities_kratky_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDEL3_kratky_img.png
pddf_plothttps://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDEL3_pofr_img.png
intensities_guinier_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDEL3_guinier_img.png
sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDEL3.sascif
experiment.instrument.detector.typeCustom
experiment.instrument.detector.nameLinear gas detector
experiment.instrument.detector.resolution605.0
experiment.instrument.nameLURE
experiment.instrument.cityOrsay
experiment.instrument.countryFrance
experiment.instrument.beamline_nameD24
experiment.instrument.beam_geometrynull
experiment.instrument.type_of_sourceX-ray synchrotron
experiment.instrument.point_sourcenull
experiment.instrument.line_collimationnull
experiment.instrument.sample_path_lengthnull
experiment.instrument.line_collimation_slitlengthnull
experiment.instrument.line_collimation_integrationwidthnull
experiment.instrument.xray_energynull
experiment.instrument.beam_profile_ahnull
experiment.instrument.beam_profile_alnull
experiment.sample.molecule[0].long_nameNeutrophil cytosol factor 2
experiment.sample.molecule[0].short_namep67phox
experiment.sample.molecule[0].sequenceGPLGSPNSARMSLVEAISLWNEGVLAADKKDWKGALDAFSAVQDPHSRICFNIGCMYTIL KNMTEAEKAFTRSINRDKHLAVAYFQRGMLYYQTEKYDLAIKDLKEALIQLRGNQLIDYK ILGLQFKLFACEVLYNIAFMYAKKEEWKKAEEQLALATSMKSEPRHSKIDKAMECVWKQK LYEPVVIPVGKLFRPNERQVAQLAKKDYLGKATVVASVVDQDSFSGFAPLQPQAAEPPPR PKTPEIFRALEGEAHRVLFGFVPETKEELQVMPGNIVFVLKKGNDNWATVMFNGQKGLVP CNYLEPVELRIHPQQQPQEESSPQSDIPAPPSSKAPGRPQLSPGQKQKEEPKEVKLSVPM PYTLKVHYKYTVVMKTQPGLPYSQVRDMVSKKLELRLEHTKLSYRPRDSNELVPLSEDSM KDAWGQVKNYCLTLWCENTVGDQGFPDEPKESEKADANNQTTEPQLKKGSQVEALFSYEA TQPEDLEFQEGDIILVLSKVNEEWLEGESKGKVGIFPKVFVEDSATTDLESTRREV
experiment.sample.molecule[0].organismHomo sapiens
experiment.sample.molecule[0].uniprot_codeP19878
experiment.sample.molecule[0].uniprot_range_first1
experiment.sample.molecule[0].uniprot_range_last526
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMSLVEAISLWNEGVLAADKKDWKGALDAFSAVQDPHSRICFNIGCMYTILKNMTEAEKAF TRSINRDKHLAVAYFQRGMLYYQTEKYDLAIKDLKEALIQLRGNQLIDYKILGLQFKLFA CEVLYNIAFMYAKKEEWKKAEEQLALATSMKSEPRHSKIDKAMECVWKQKLYEPVVIPVG KLFRPNERQVAQLAKKDYLGKATVVASVVDQDSFSGFAPLQPQAAEPPPRPKTPEIFRAL EGEAHRVLFGFVPETKEELQVMPGNIVFVLKKGNDNWATVMFNGQKGLVPCNYLEPVELR IHPQQQPQEESSPQSDIPAPPSSKAPGRPQLSPGQKQKEEPKEVKLSVPMPYTLKVHYKY TVVMKTQPGLPYSQVRDMVSKKLELRLEHTKLSYRPRDSNELVPLSEDSMKDAWGQVKNY CLTLWCENTVGDQGFPDEPKESEKADANNQTTEPQLKKGSQVEALFSYEATQPEDLEFQE GDIILVLSKVNEEWLEGECKGKVGIFPKVFVEDCATTDLESTRREV
experiment.sample.molecule[0].mw60.666
experiment.sample.molecule[0].total_mw60.666
experiment.sample.molecule[0].number_molecules1
experiment.sample.molecule[0].complex_stateFalse
experiment.sample.molecule[0].deuterationnull
experiment.sample.molecule[0].molecule_sourcebiological
experiment.sample.molecule[0].molecule_descriptionnull
experiment.sample.buffer.name20 mM HEPES, 50 mM NaCl, 1 mM EDTA, 2 mM DTT, 5% glycerol
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph8.0
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameThe neutrophil cytosol factor 2 (p67phox) subunit of phagocyte NADPH oxidase
experiment.sample.ext_coefficientnull
experiment.sample.contrastnull
experiment.sample.specific_volnull
experiment.sample.dry_volnull
experiment.sample.absorbptionnull
experiment.sample.deuterationnull
experiment.sample.mixturenull
experiment.contributor[0].affiliation[0].short_namenull
experiment.contributor[0].affiliation[0].addressParis, France
experiment.contributor[0].affiliation[0].full_nameI2BC-CNRS
experiment.contributor[0].affiliation[0].webpagehttp://www.i2bc.paris-saclay.fr
experiment.contributor[0].contributor_nameDominique
experiment.contributor[0].contributor_surnameDURAND
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2003-04-09
experiment.storage_temperature4.0
experiment.cell_temperature4.0
experiment.exposure_time200.0
experiment.number_of_frames8
experiment.wavelength0.1488
experiment.sample_detector_distance1.378
experiment.concentration_min0.3
experiment.concentration_max3.8
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.148
experiment.s_max3.374
experiment.total_exposure_timenull
experiment.seccolumnnull
fits[0].models[0].model_plothttps://www.sasbdb.org/media/pdb_file/images/SASDEL3_fit1_model1_img.png
fits[0].models[0].softwareCustom in-house
fits[0].models[0].pdb_link[]
fits[0].models[0].model_titlenull
fits[0].models[0].type_of_modelatomic
fits[0].models[0].software_versionnull
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fits[0].models[0].model_mw63.06
fits[0].models[0].bead_radiusnull
fits[0].models[0].lognull
fits[0].models[0].symmetrynull
fits[0].models[0].commentnull
fits[0].models[0].user262
fits[0].fit_unit1/A
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fits[0].softwareBUNCH
fits[0].chi_square_value1.304
fits[0].p_value1e-06
fits[0].fit_residual_plotfit4columns1678_fitresiduals_img.png
fits[0].fit_datahttps://www.sasbdb.org/media/fitting_files/SASDEL3_fit1.fit
fits[0].fit_loghttps://www.sasbdb.org/media/fitting_files/log_files/p67_Model00.log
fits[0].software_version08
fits[0].descriptionp67phox in solution: Comparison of the experimental data (blue dots) with the calculated scattering pattern (red line) of the BUNCH model shown on the rightchi2=1.304. The ultimate adjustment shown here was performed using the program CRYSOL.
fits[1].models[]
fits[1].fit_unit1/A
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fits[1].softwareEOM/GAJOE
fits[1].chi_square_value0.828
fits[1].p_value0.493356
fits[1].fit_residual_plotfit4columns1679_fitresiduals_img.png
fits[1].fit_datahttps://www.sasbdb.org/media/fitting_files/SASDEL3_fit2.fit
fits[1].fit_lognull
fits[1].software_version2.1
fits[1].descriptionThe fitting to the experimental curve using EOM program. This good fit with our experimental intensities chi2=0.828) was obtained only when using the “compact” reconstructed linkers.
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of the p67phox subunit of phagocyte NADPH oxidase in 20 mM HEPES, 50 mM NaCl, 1 mM EDTA, 2 mM DTT, 5% glycerol, pH 8 were collected on the D24 beam line at the LURE storage ring (Orsay, France) using a linear gas home-made detector at a sample-detector distance of 1.4 m and at a wavelength of λ = 0.1488 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). Samples were studied at different concentrations ranging from 0.3 to 3.8 mg/ml measured at 4°C. Eight successive 200 second frames were collected. SAXS data were normalized to the intensity of the incident beam, averaged and background subtracted using the program package PRIMUS. Intensities were put on an absolute scale (cm-1) using water scattering. The final pattern used for fitting was obtained by extrapolating to infinite dilution of the set of curves recorded at the different concentrations. Molecular mass was obtained using the bayesian inference approach proposed in PRIMUS/qt, which combines four concentration independent MM estimators: M=62.4 kDa within the credibility interval [60.2-67.9].
tags[]
intensity_unit1/cm
experimental_mw62.4
experimental_mw_errornull
guinier_i0_mw60.4
guinier_i0_mw_error6.0
porod_mw75.3
porod_mw_errornull
pddf_i00.05088
pddf_i0_error0.0006
guinier_i00.05
guinier_i0_error0.0006
pddf_rg4.54
pddf_rg_error0.1
guinier_rg4.27
guinier_rg_error0.1
pddf_dmax16.0
pddf_dmax_error1.0
porod_volume113.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first1
guinier_point_last8
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDEL3_datloglog_img.png
symmetrynull
last_modified2020-08-28T15:27:52.342524+02:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDEL3
statussuccess
started_at2026-08-11T14:02:41.380130+00:00
finished_at2026-08-11T14:02:49.689847+00:00
source_last_modified2020-08-28T15:27:52.342524+02:00
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View the complete summary.json source
{
  "code": "SASDEL3",
  "status": "Published",
  "type_of_curve": "Extrapolated to infinite dilution",
  "angular_unit": "1/A",
  "project": {
    "title": "Quantitative live-cell imaging and 3D modeling reveal critical functional features in the cytosolic complex of phagocyte NADPH oxidase.",
    "publication": {
      "title": "Quantitative live-cell imaging and 3D modeling reveal critical functional features in the cytosolic complex of phagocyte NADPH oxidase.",
      "author_list": "Ziegler CS, Bouchab L, Tramier M, Durand D, Fieschi F, Dupré-Crochet S, Mérola F, Nüße O, Erard M",
      "journal": "J Biol Chem",
      "doi": "10.1074/jbc.RA118.006864",
      "pmid": "30630949",
      "published_date": "2019 Jan 10"
    },
    "status": "released",
    "submitted_date": "2018-08-28",
    "released_date": "2019-01-16"
  },
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  "intensities_data": "https://www.sasbdb.org/media/intensities_files/SASDEL3.dat",
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  "pddf_plot": "https://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDEL3_pofr_img.png",
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  "experiment": {
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      "detector": {
        "type": "Custom",
        "name": "Linear gas detector",
        "resolution": 605.0
      },
      "name": "LURE",
      "city": "Orsay",
      "country": "France",
      "beamline_name": "D24",
      "beam_geometry": null,
      "type_of_source": "X-ray synchrotron",
      "point_source": null,
      "line_collimation": null,
      "sample_path_length": null,
      "line_collimation_slitlength": null,
      "line_collimation_integrationwidth": null,
      "xray_energy": null,
      "beam_profile_ah": null,
      "beam_profile_al": null
    },
    "sample": {
      "molecule": [
        {
          "long_name": "Neutrophil cytosol factor 2",
          "short_name": "p67phox",
          "sequence": "GPLGSPNSARMSLVEAISLWNEGVLAADKKDWKGALDAFSAVQDPHSRICFNIGCMYTIL\r\nKNMTEAEKAFTRSINRDKHLAVAYFQRGMLYYQTEKYDLAIKDLKEALIQLRGNQLIDYK\r\nILGLQFKLFACEVLYNIAFMYAKKEEWKKAEEQLALATSMKSEPRHSKIDKAMECVWKQK\r\nLYEPVVIPVGKLFRPNERQVAQLAKKDYLGKATVVASVVDQDSFSGFAPLQPQAAEPPPR\r\nPKTPEIFRALEGEAHRVLFGFVPETKEELQVMPGNIVFVLKKGNDNWATVMFNGQKGLVP\r\nCNYLEPVELRIHPQQQPQEESSPQSDIPAPPSSKAPGRPQLSPGQKQKEEPKEVKLSVPM\r\nPYTLKVHYKYTVVMKTQPGLPYSQVRDMVSKKLELRLEHTKLSYRPRDSNELVPLSEDSM\r\nKDAWGQVKNYCLTLWCENTVGDQGFPDEPKESEKADANNQTTEPQLKKGSQVEALFSYEA\r\nTQPEDLEFQEGDIILVLSKVNEEWLEGESKGKVGIFPKVFVEDSATTDLESTRREV",
          "organism": "Homo sapiens",
          "uniprot_code": "P19878",
          "uniprot_range_first": 1,
          "uniprot_range_last": 526,
          "oligomerization": "monomer",
          "molecular_type": "protein",
          "uniprot_sequence": "MSLVEAISLWNEGVLAADKKDWKGALDAFSAVQDPHSRICFNIGCMYTILKNMTEAEKAF\nTRSINRDKHLAVAYFQRGMLYYQTEKYDLAIKDLKEALIQLRGNQLIDYKILGLQFKLFA\nCEVLYNIAFMYAKKEEWKKAEEQLALATSMKSEPRHSKIDKAMECVWKQKLYEPVVIPVG\nKLFRPNERQVAQLAKKDYLGKATVVASVVDQDSFSGFAPLQPQAAEPPPRPKTPEIFRAL\nEGEAHRVLFGFVPETKEELQVMPGNIVFVLKKGNDNWATVMFNGQKGLVPCNYLEPVELR\nIHPQQQPQEESSPQSDIPAPPSSKAPGRPQLSPGQKQKEEPKEVKLSVPMPYTLKVHYKY\nTVVMKTQPGLPYSQVRDMVSKKLELRLEHTKLSYRPRDSNELVPLSEDSMKDAWGQVKNY\nCLTLWCENTVGDQGFPDEPKESEKADANNQTTEPQLKKGSQVEALFSYEATQPEDLEFQE\nGDIILVLSKVNEEWLEGECKGKVGIFPKVFVEDCATTDLESTRREV",
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          "total_mw": 60.666,
          "number_molecules": 1,
          "complex_state": false,
          "deuteration": null,
          "molecule_source": "biological",
          "molecule_description": null
        }
      ],
      "buffer": {
        "name": "20 mM HEPES, 50 mM NaCl, 1 mM EDTA, 2 mM DTT, 5% glycerol",
        "concentration_unit": null,
        "comment": null,
        "additive": null,
        "concentration": null,
        "pka": null,
        "ph": 8.0,
        "deuteration": null
      },
      "purity_method": null,
      "name": "The neutrophil cytosol factor 2 (p67phox) subunit of phagocyte NADPH oxidase",
      "ext_coefficient": null,
      "contrast": null,
      "specific_vol": null,
      "dry_vol": null,
      "absorbption": null,
      "deuteration": null,
      "mixture": null
    },
    "contributor": [
      {
        "affiliation": [
          {
            "short_name": null,
            "address": "Paris, France",
            "full_name": "I2BC-CNRS",
            "webpage": "http://www.i2bc.paris-saclay.fr"
          }
        ],
        "contributor_name": "Dominique",
        "contributor_surname": "DURAND",
        "orcid": null
      }
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    "concentration_method": null,
    "concentration_unit": null,
    "date": "2003-04-09",
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    "wavelength": 0.1488,
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    "flow_rate": null,
    "s_min": 0.148,
    "s_max": 3.374,
    "total_exposure_time": null,
    "seccolumn": null
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      "models": [
        {
          "model_plot": "https://www.sasbdb.org/media/pdb_file/images/SASDEL3_fit1_model1_img.png",
          "software": "Custom in-house",
          "pdb_link": [],
          "model_title": null,
          "type_of_model": "atomic",
          "software_version": null,
          "model_data": "https://www.sasbdb.org/media/pdb_file/SASDEL3_fit1_model1.pdb",
          "model_mw": 63.06,
          "bead_radius": null,
          "log": null,
          "symmetry": null,
          "comment": null,
          "user": 262
        }
      ],
      "fit_unit": "1/A",
      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/SASDEL3_fit1_fixed_fit_img.png",
      "software": "BUNCH",
      "chi_square_value": 1.304,
      "p_value": 1e-06,
      "fit_residual_plot": "fit4columns1678_fitresiduals_img.png",
      "fit_data": "https://www.sasbdb.org/media/fitting_files/SASDEL3_fit1.fit",
      "fit_log": "https://www.sasbdb.org/media/fitting_files/log_files/p67_Model00.log",
      "software_version": "08",
      "description": "p67phox in solution: \r\nComparison of the experimental data (blue dots) with the calculated scattering pattern (red line) of the BUNCH model shown on the rightchi2=1.304. The ultimate adjustment shown here was performed using the program CRYSOL."
    },
    {
      "models": [],
      "fit_unit": "1/A",
      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/SASDEL3_fit2_fixed_fit_img.png",
      "software": "EOM/GAJOE",
      "chi_square_value": 0.828,
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      "fit_residual_plot": "fit4columns1679_fitresiduals_img.png",
      "fit_data": "https://www.sasbdb.org/media/fitting_files/SASDEL3_fit2.fit",
      "fit_log": null,
      "software_version": "2.1",
      "description": "The fitting to the experimental curve using EOM program. This good fit with our experimental intensities chi2=0.828) was obtained only when using the “compact” reconstructed linkers."
    }
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  "pddf_software": "ATSAS GNOM",
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  "i0_calibration_standard": null,
  "description": null,
  "experiment_description": "Synchrotron SAXS data from solutions of the p67phox subunit of phagocyte NADPH oxidase in 20 mM HEPES, 50 mM NaCl, 1 mM EDTA, 2 mM DTT, 5% glycerol, pH 8 were collected on the D24 beam line at the LURE storage ring (Orsay, France) using a linear gas home-made detector at a sample-detector distance of 1.4 m and at a wavelength of λ = 0.1488 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). Samples were studied at different concentrations ranging from 0.3 to 3.8 mg/ml measured at 4°C. Eight successive 200 second frames were collected. SAXS data were normalized to the intensity of the incident beam, averaged and background subtracted using the program package PRIMUS. Intensities were put on an absolute scale (cm-1) using water scattering. The final pattern used for fitting was obtained by extrapolating to infinite dilution of the set of curves recorded at the different concentrations. Molecular mass was obtained using the bayesian inference approach proposed in PRIMUS/qt, which combines four concentration independent MM estimators: M=62.4 kDa within the credibility interval [60.2-67.9].",
  "tags": [],
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  "i0_calibration_standard_data": null,
  "intensities_log_log_plot": "SASDEL3_datloglog_img.png",
  "symmetry": null,
  "last_modified": "2020-08-28T15:27:52.342524+02:00",
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}
View the complete manifest.json source
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